Schumann Benjamin, Hahm Heung Sik, Parameswarappa Sharavathi G, Reppe Katrin, Wahlbrink Annette, Govindan Subramanian, Kaplonek Paulina, Pirofski Liise-Anne, Witzenrath Martin, Anish Chakkumkal, Pereira Claney L, Seeberger Peter H
Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1, 14424 Potsdam, Germany.
Freie Universität Berlin, Arnimallee 22, 14195 Berlin, Germany.
Sci Transl Med. 2017 Mar 8;9(380). doi: 10.1126/scitranslmed.aaf5347.
Glycoconjugate vaccines based on capsular polysaccharides (CPSs) of pathogenic bacteria such as successfully protect from disease but suffer from incomplete coverage, are troublesome to manufacture from isolated CPSs, and lack efficacy against certain serotypes. Defined, synthetic oligosaccharides are an attractive alternative to isolated CPSs but require the identification of immunogenic and protective oligosaccharide antigens. We describe a medicinal chemistry strategy based on a combination of automated glycan assembly (AGA), glycan microarray-based monoclonal antibody (mAb) reverse engineering, and immunological evaluation in vivo to uncover a protective glycan epitope (glycotope) for serotype 8 (ST8). All four tetrasaccharide frameshifts of ST8 CPS were prepared by AGA and used in glycan microarray experiments to identify the glycotopes recognized by antibodies against ST8. One tetrasaccharide frameshift that was preferentially recognized by a protective, CPS-directed mAb was conjugated to the carrier protein CRM197. Immunization of mice with this semisynthetic glycoconjugate followed by generation and characterization of a protective mAb identified protective and nonprotective glycotopes. Immunization of rabbits with semisynthetic ST8 glycoconjugates containing protective glycotopes induced an antibacterial immune response. Coformulation of ST8 glycoconjugates with the marketed 13-valent glycoconjugate vaccine Prevnar 13 yielded a potent 14-valent vaccine. Our strategy presents a facile approach to develop efficient semisynthetic glycoconjugate vaccines.
基于致病细菌荚膜多糖(CPS)的糖缀合物疫苗,如 ,能成功预防疾病,但存在覆盖不完整、从分离的CPS制造麻烦以及对某些血清型缺乏效力等问题。明确的合成寡糖是分离CPS的有吸引力的替代物,但需要鉴定免疫原性和保护性寡糖抗原。我们描述了一种基于自动聚糖组装(AGA)、聚糖微阵列单克隆抗体(mAb)逆向工程和体内免疫学评估相结合的药物化学策略,以发现8型血清型(ST8)的保护性聚糖表位(糖表位)。ST8 CPS的所有四个四糖移码突变体均通过AGA制备,并用于聚糖微阵列实验,以鉴定被抗ST8抗体识别的糖表位。一种优先被保护性的、针对CPS的mAb识别的四糖移码突变体与载体蛋白CRM197偶联。用这种半合成糖缀合物免疫小鼠,随后产生并表征保护性mAb,确定了保护性和非保护性糖表位。用含有保护性糖表位的半合成ST8糖缀合物免疫兔子诱导了抗菌免疫反应。将ST8糖缀合物与市售的13价糖缀合物疫苗沛儿13联合配方,产生了一种有效的14价疫苗。我们的策略为开发高效的半合成糖缀合物疫苗提供了一种简便的方法。